KANSL1 - Koolen-de Vries syndrome

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Koolen-De Vries syndrome
  • Conditions > Multiple congenital anomalies (MCA) > Koolen-De Vries syndrome

This product is also part of the following panels:

  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Orofacial clefting panel with genome wide CNV analysis

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
Remarks
Deletions can be detected by SNP array analysis

OMIM: 612452
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 443
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Gene

KANSL1 - Koolen-de Vries syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 443
View Add

KANSL1 - Koolen-de Vries syndrome


€ 443
Add